Melpida: Recombinant Adeno-associated Virus (Serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt)
Recruiting
Phase 1
Phase 2
Interventional Study
Spasticity, Muscle
Microcephaly
Intellectual Deficiency
Growth Retardation
SPG50
Spastic Paraplegia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 4 Months – 10
- Sex
- Any
- Trial phase
- Phase 1/2
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 4 (estimated)
- Sponsor
- Elpida Therapeutics SPC · Industry
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About This Trial
MELPIDA is proposed for the treatment of subjects with SPG50 and targets neuronal cells to deliver a fully functional human AP4M1 cDNA copy via intrathecal injection to counter the associated neuronal loss. Outcomes will evaluate the safety and tolerability of a single dose of MELPIDA, which will be measured by the treatment-associated adverse events (AEs) and serious adverse events (SAEs). Second…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Age 4 months-10 years old
2. Confirmed diagnosis of SPG50 disease by:
1. Genomic DNA mutation analysis demonstrating homozygous or compound heterozygous, confirmed pathogenic variants in the AP4M1 gene
2. Clinical history or examination features consistent with SPG50 a…
Contacts